drugset / Trial / NCT00405587

Safety Study of PLX4032 in Patients With Solid Tumors

NCT00405587

Phase 1 Completed 109 enrolled Plexxikon Roche Pharma AG · collab
NaSingle-groupOpen-labelTreatment

Summary

The primary objective of this FIH study is to assess the safety and pharmacokinetics of PLX4032 in patients with solid tumors. The secondary objective is to assess the pharmacodynamic activity in paired biopsy specimens obtained from patients with malignant melanoma who have the V600E BRAF oncogenic mutation.

Timeline

Start
2006-11
Primary completion
2015-07
Completion
2016-02

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Vemurafenib Small molecule 240 mg Oral
Subject Vemurafenib Small molecule 960 mg Oral
Subject Vemurafenib Small molecule 1120 mg Oral